Product Details

SNP ID

rs140964607

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:159808339 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAAAACCAGACTCTGTCCATGGGA[A/G]CAGCAACAGTGCAGAGCCGTGGCCA

Phenotype

MIM: 613562

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FCRL6 PubMed Links

Gene Details

Gene

FCRL6

Gene Name

Fc receptor like 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004310.2	332	Missense Mutation	ACA,GCA	T72A	NP_001004310.2
NM_001284217.1	332	Missense Mutation	ACA,GCA	T79A	NP_001271146.1
XM_005245128.3	332	Missense Mutation	ACA,GCA	T82A	XP_005245185.1
XM_005245129.3	332	Missense Mutation	ACA,GCA	T67A	XP_005245186.1
XM_005245131.3	332	Missense Mutation	ACA,GCA	T82A	XP_005245188.1
XM_006711292.3	332	Missense Mutation	ACA,GCA	T82A	XP_006711355.1
XM_011509480.1	332	Missense Mutation	ACA,GCA	T79A	XP_011507782.1
XM_011509481.2	332	Missense Mutation	ACA,GCA	T82A	XP_011507783.1
XM_017001176.1	332	Missense Mutation	ACA,GCA	T35A	XP_016856665.1
XM_017001177.1	332	Missense Mutation	ACA,GCA	T3A	XP_016856666.1

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